Evidence map›Paper›PMID 35455041›Full record

ArticleLife (Basel, Switzerland)2022

Identification of Cell Markers and Their Expression Patterns in Skin Based on Single-Cell RNA-Sequencing Profiles.

Xianchao Zhou, Shijian Ding, Deling Wang, Lei Chen, Kaiyan Feng, Tao Huang, Zhandong Li, Yudong Cai

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.5field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 26 citations in OpenAlex.

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  10. Characterization of spleen and lymph node cell typesFrontiers in molecular neuroscience · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 1 country.

Xianchao ZhouSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
Shijian DingSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
Deling WangState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Department of Medical Imaging, Sun Yat-sen University Cancer Center, Guangzhou 510060, China.
Lei ChenCollege of Information Engineering, Shanghai Maritime University, Shanghai 201306, China.ORCID 0000-0003-3068-1583
Kaiyan FengDepartment of Computer Science, Guangdong AIB Polytechnic College, Guangzhou 510507, China.
Tao HuangBio-Med Big Data Center, CAS Key Laboratory of Computational Biology, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200031, China.ORCID 0000-0003-1975-9693
Zhandong LiCollege of Food Engineering, Jilin Engineering Normal University, Changchun 130052, China.
Yudong CaiSchool of Life Sciences, Shanghai University, Shanghai 200444, China.ORCID 0000-0001-5664-7979
Shanghai University · CNGuangdong Polytechnic Normal University · CNJilin Engineering Normal University · CNShanghai Institute of Nutrition and Health · CNShanghai Maritime University · CNSun Yat-sen University · CN

Funding

Fund of the Key Laboratory of Tissue Microenvironment and Tumor of Chinese Academy of Sciences 202002National Key R&D Program of China 2018YFC0910403Strategic Priority Research Program of Chinese Academy of Sciences XDA26040304Strategic Priority Research Program of Chinese Academy of Sciences XDB38050200
6 · The paper itself

Abstract

Atopic dermatitis and psoriasis are members of a family of inflammatory skin disorders. Cellular immune responses in skin tissues contribute to the development of these diseases. However, their underlying immune mechanisms remain to be fully elucidated. We developed a computational pipeline for analyzing the single-cell RNA-sequencing profiles of the Human Cell Atlas skin dataset to investigate the pathological mechanisms of skin diseases. First, we applied the maximum relevance criterion and the Boruta feature selection method to exclude irrelevant gene features from the single-cell gene expression profiles of inflammatory skin disease samples and healthy controls. The retained gene features were ranked by using the Monte Carlo feature selection method on the basis of their importance, and a feature list was compiled. This list was then introduced into the incremental feature selection method that combined the decision tree and random forest algorithms to extract important cell markers and thus build excellent classifiers and decision rules. These cell markers and their expression patterns have been analyzed and validated in recent studies and are potential therapeutic and diagnostic targets for skin diseases because their expression affects the pathogenesis of inflammatory skin diseases.

Indexed as

cell markerclassification algorithmexpression patternfeature selectionrule learningskin disease

Identifiers

PMID35455041
PMCPMC9025372
OpenAlexW4224248258

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.